Canonical Allele Identifier: CA2840868056
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104014dup , CM000681.2:g.1104014dup GRCh38
NC_000019.9:g.1104013dup , CM000681.1:g.1104013dup GRCh37
NC_000019.8:g.1055013dup NCBI36
NG_050621.1:g.5089dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000706713.1:c.-30dup ENSP00000516510.1:n.-30dup
ENST00000354171.13:c.-30dup MANE Select ENSP00000346103.7:n.-30dup
ENST00000589115.6:c.-30dup ENSP00000466872.3:n.-30dup
ENST00000354171.12:c.-30dup ENSP00000346103.7:n.-30dup
ENST00000589115.5:c.-30dup ENSP00000466872.2:n.-30dup
ENST00000616066.4:c.-30dup ENSP00000485000.1:n.-30dup
NM_001039847.2:c.-30dup NP_001034936.1:n.-30dup
NM_002085.4:c.-30dup NP_002076.2:n.-30dup
NM_001039847.3:c.-30dup NP_001034936.1:n.-30dup
NM_002085.5:c.-30dup MANE Select NP_002076.2:n.-30dup